Tag | Content |
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EnhancerAtlas ID | HS116-07494 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:290580-292070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr12:291882-291893 | CTAATCCCCTT | - | 6.32 | ZNF263 | MA0528.1 | chr12:291625-291646 | TCCTCCCCTGCGCCCTCCCTC | - | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 291440 | 291523 | chr12 | 291572 | 292069 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I000182 | chr12 | 291400 | 292062 |
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Enhancer Sequence | ACTGCAGGTG TGCACCACTA TGCCTGAATA ATTTTTGTTT GTCTTTGTAG AGACGGAGTC 60 TCACTACGTT GCCCAGGCTG GTCTCAAACT CCTGGCCTCA AGGGATCCAC CCACCTCGGC 120 CTAGGCTTGC CATTTTTAAA TAATGGAATG GACTCCATGG CCTATTGCAC AGCAGTCCCA 180 AGGAGTCCAG GGGCTAACAG CCTTTCACGT CTCAGCGTGA ACCCCACAGA ACGGAAGTGA 240 GATTGATTTC TCCTTCAGGG GGCTGGCACT ACATGGCTGC GGCCCTCGGC ATGCCCCCTC 300 CCATCCCAGC TCTGACAGAT GTGGCCAATT GATCACTGCT TTCTGGGAGT CACCATCAAT 360 CACATGTGCT GACTCCAGGA TGAAAGAACT TGCCAACCGC CCCGTGGTGT CCTCATGGAG 420 ACACCTGGAA GGAAGGCATT TTGACGGGAG GTAGCTTAGA GCAGGGGGCA GCAGGCGGGA 480 GGTGTGGCCC TCCTAGTGCC ACTGCTCTCA GGTCACTTGC GGACAGCAGC TCTGGGGGTG 540 CTGGCTTTGG CTCCTTAGCT CTGCCGCTCA GGGACTCAGG GCTGCTTCCT GCCAGGACTC 600 CTCACTACTC AGCAACCGGT CGACTACCCT GTGCACCAGG TCCCCTCACT CACCTTCCTC 660 GGGGTGAGCC ACATGGCCCC CGGTGTCACA GATGAAGGTC TGAAGACGCC CAGGCAAGAA 720 GGACGCTCCG TCCAGGGCGG AGCCTTGGGA GCAAAGGCAG ACCCCGTGGA GGGCAAGGGA 780 GGTGGTCCTT CCAGGAGAAC GTGAGGCCCA GCCAGCGCCC AGCGGCCTGG AGCCGCAGGC 840 TGAGTTCTGA TCTGCTCCCC TTCCCGTCCC AGGACGGCAG CCAGGCCCCA AGATAGACCA 900 AGCCCAGGTC AGAGTCAGGG AGGTTAAATG AGGGCGCAGG AATGGGGGGT GCAGAGGGAC 960 AGGTCCAGAA GTGGTTCTGC CAGAATTCCC TTCTGGATGG GCTGGAGGAG AGGGAGCTGG 1020 AGCTCAGCGG GTGGGCGGAG TGCTCTCCTC CCCTGCGCCC TCCCTCCCGT GCCCCTGCAG 1080 GGCTGCACGG GTTCCCTCCC TAGGGAACCA GGCTGCCTAA CCCACCAGCC GGCCCCTAGC 1140 ACCTCAGCGC TTCCTGCTCC CATGACCCTA AGGACTAAGT GACCTCAAGC CTGGCTCTGG 1200 GAAAACTGTG GGAACCGGCT GCTGGGAAGA CGACCTGGCT GTTACTCCCA CGTTTCCAAC 1260 TGCCTAGACA GACCTGCCCT GCCCTCCTTT CCTCAAGAAA CCCTAATCCC CTTTCCTTCT 1320 GAGACATCTA GGGTAGGAGT CAGCCTCCCT CCCTGCACCC TCAGAGGGAA TGGAAGGCAG 1380 GGGAGTCATA CAGCAGTGCC AGGCCTGCAG GCTGAGTCAC AGGCCAGTCA TCCTTCTATG 1440 GCTAAGGGGA CTACTTCACT TAAGAGGTTA AAAAAGAAGA ACAGAATAAG 1490
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